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癫痫相关认知功能障碍的遗传和分子基础。

Genetic and molecular basis of epilepsy-related cognitive dysfunction.

机构信息

Department of Neurology, First Affiliated Hospital, Kunming Medical University, 295 Xi Chang Road, Kunming, Yunnan 650032, PR China.

Biomedicine Engineering Research Center, Kunming Medical University, 1168 Chun Rong West Road, Kunming, Yunnan 650500, PR China.

出版信息

Epilepsy Behav. 2020 Mar;104(Pt A):106848. doi: 10.1016/j.yebeh.2019.106848. Epub 2020 Feb 3.

Abstract

Epilepsy is a common neurological disease characterized by recurrent seizures. About 70 million people were affected by epilepsy or epileptic seizures. Epilepsy is a complicated complex or symptomatic syndromes induced by structural, functional, and genetic causes. Meanwhile, several comorbidities are accompanied by epileptic seizures. Cognitive dysfunction is a long-standing complication associated with epileptic seizures, which severely impairs quality of life. Although the definitive pathogenic mechanisms underlying epilepsy-related cognitive dysfunction remain unclear, accumulating evidence indicates that multiple risk factors are probably involved in the development and progression of cognitive dysfunction in patients with epilepsy. These factors include the underlying etiology, recurrent seizures or status epilepticus, structural damage that induced secondary epilepsy, genetic variants, and molecular alterations. In this review, we summarize several theories that may explain the genetic and molecular basis of epilepsy-related cognitive dysfunction.

摘要

癫痫是一种常见的神经系统疾病,其特征是反复发作。大约有 7000 万人受到癫痫或癫痫发作的影响。癫痫是由结构、功能和遗传原因引起的复杂的综合征或症状性疾病。同时,癫痫发作伴有多种合并症。认知功能障碍是癫痫相关的长期并发症,严重影响生活质量。尽管癫痫相关认知功能障碍的确切发病机制尚不清楚,但越来越多的证据表明,多种危险因素可能参与癫痫患者认知功能障碍的发展和进展。这些因素包括潜在病因、反复发作或癫痫持续状态、导致继发性癫痫的结构损伤、遗传变异和分子改变。在这篇综述中,我们总结了一些可能解释癫痫相关认知功能障碍的遗传和分子基础的理论。

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